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. 2010 Feb 2;119(5):617–630. doi: 10.1007/s00401-010-0644-7

Fig. 6.

Fig. 6

The CDV fusogenic complexes are potentially functional in DBCCs. a, b Both CDV surface glycoproteins are properly expressed in glial cells. DBCCs were infected with rA75/17red with an MOI of 0.01. Merged images of both glycoproteins F and H stained with anti-F and anti-H antibodies, respectively, followed by secondary alexa fluor 488-conjugated antibody (green) and astrocytes labeled using an anti-GFAP antibody, followed by a secondary alexa fluor 555-conjugated antibody (red). Confocal laser microscopy ×200. c, d F/H complexes are cell surface targeted in potentially functional. Prior to infection of DBCCs with rA75/17red (MOI of 0.01), cells were transduced with a lentivirus vector expressing SLAM (pRRL-SLAM) or with a control empty plasmid (pRRL). Syncytia formation was readily observed in CDV-infected cells. No syncytia are demonstrated in the control culture